Convenient Palladium-Catalyzed Arsination: Direct Synthesis of Functionalized Aryl Arsines, Optically Active As,N Ligands, and Their Metal Complexes-Reference-Cited by-同舟云学术

Convenient Palladium-Catalyzed Arsination: Direct Synthesis of Functionalized Aryl Arsines, Optically Active As,N Ligands, and Their Metal Complexes

Published:2005-07-16 Issue:17 Volume:24 Page:4170-4178
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Kwong Fuk Yee¹,Lai Chi Wai¹,Yu Michael¹,Tan Duan-Ming¹,Lam Fuk Loi¹,Chan Albert S. C.¹,Chan Kin Shing¹

Affiliation:

1. Department of Chemistry and Open Laboratory of Chirotechnology of the Institute of Molecular Technology for Drug Discovery and Synthesis, The Chinese University of Hong Kong, Shatin, New Territories, Hong Kong, China, and Department of Applied Biology and Chemical Technology, The Hong Kong Polytechnic University, Hung Hom, Kowloon, Hong Kong, China

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om050237%2B

Reference69 articles.

1. Large rate accelerations in the stille reaction with tri-2-furylphosphine and triphenylarsine as palladium ligands: mechanistic and synthetic implications

2. C-Glycosides and C-disaccharide precursors through carbonylative Stille coupling reactions

3. Stille Coupling Reaction Using 4-(Trimethylsilyl)-2-butenylstannanes To Afford Allylic Silanes

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